Skip to main content
Advertisement
  • Loading metrics

Influenza-associated hospitalisation and mortality rates among global Indigenous populations; a systematic review and meta-analysis

  • Juliana M. Betts,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Visualization, Writing – original draft, Writing – review & editing

    Affiliation School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia

  • Aaron L. Weinman,

    Roles Data curation, Validation, Writing – review & editing

    Affiliation Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

  • Jane Oliver,

    Roles Formal analysis, Writing – review & editing

    Affiliation Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

  • Maxwell Braddick,

    Roles Formal analysis, Visualization, Writing – review & editing

    Affiliations Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia, Victorian Infectious Disease Service, The Royal Melbourne Hospital at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

  • Siyu Huang,

    Roles Data curation, Formal analysis, Writing – review & editing

    Affiliations Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia, Melbourne Medical School, University of Melbourne, Melbourne, Australia

  • Matthew Nguyen,

    Roles Data curation, Writing – review & editing

    Affiliation Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

  • Adrian Miller,

    Roles Writing – review & editing

    Affiliation Centre for Indigenous Health Equity Research, Central Queensland University, Townsville, Australia

  • Steven Y. C. Tong,

    Roles Conceptualization, Formal analysis, Methodology, Supervision, Writing – review & editing

    Affiliations Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia, Victorian Infectious Disease Service, The Royal Melbourne Hospital at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

  • Katherine B. Gibney

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Supervision, Writing – review & editing

    katherine.gibney@unimelb.edu.au

    Affiliations Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia, Victorian Infectious Disease Service, The Royal Melbourne Hospital at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

Abstract

Background

More than 50 million influenza infections and over 100,000 deaths from influenza occur annually. While Indigenous populations experience an inequitable influenza burden, the magnitude of this inequity has not previously been estimated on a global scale. This study compared rates of influenza-associated hospitalisation and mortality between Indigenous and non-Indigenous populations globally.

Methods

A systematic review and meta-analysis was conducted including literature published prior to 13 July 2021. Eligible articles either reported a rate ratio (RR) comparing laboratory-confirmed influenza-associated hospitalisation and/or mortality between an Indigenous population and a corresponding benchmark population, or reported sufficient information for this to be calculated using publicly available data. Findings were reported by country/region and pooled by country and period (pandemic/seasonal) when multiple studies were available using a random-effects model. The I2 statistic assessed variability between studies.

Results

Thirty-six studies (moderate/high quality) were included; all from high or high-middle income countries. The pooled influenza-associated hospitalisation RR (HRR) for indigenous compared to benchmark populations was 5·7 (95% CI: 2·7–12·0) for Canada, 5·2 (2.9–9.3) for New Zealand, and 5.2 (4.2–6.4) for Australia. Of the Australian studies, the pooled HRR for seasonal influenza was 3.1 (2·7–3·5) and for pandemic influenza was 6·2 (5·1–7·5). Heterogeneity was slightly higher among studies of pandemic influenza than seasonal influenza. The pooled mortality RR was 4.1 (3·0–5.7) in Australia and 3·3 (2.7–4.1) in the United States.

Conclusions

Ethnic inequities in severe influenza persist and must be addressed by reducing disparities in the underlying determinants of health. Influenza surveillance systems worldwide should include Indigenous status to determine the extent of the disease burden among Indigenous populations. Ethnic inequities in pandemic influenza illustrate the need to prioritise Indigenous populations in pandemic response plans.

Introduction

Influenza viruses and their pandemic potential remain a persistent threat to global health in the 21st century. Typically manifesting as fever and cough, influenza can rapidly progress to more severe illness resulting in hospitalisation and death, especially among children and the elderly [1]. The Global Burden of Disease Study estimated that in 2017 influenza caused 54.5 million lower respiratory tract infections; 8.2 million of which were severe and around 145,000 subsequent deaths occurred [2]. Indigenous populations, in particular, are known to be inequitably overrepresented in the influenza disease burden [3,4] although a systematic review demonstrating the extent of this inequity on a global scale is lacking. A greater understanding of those populations most at-risk of severe influenza is required to direct prevention and intervention strategies effectively, in keeping with the Public Health Research Agenda for Influenza developed by the World Health Organization (WHO) Global Influenza Program [5].

The term ‘Indigenous’ cannot be universally defined, due to the significant diversity present among the 370 million Indigenous people living in over 70 countries throughout the world today [6]. However, the term is generally interpreted to mean peoples who have a “historical continuity with pre-invasion and pre-colonial societies” [7], with communities having the right to self-identify as Indigenous “in accordance with their customs and traditions” [8].

In general, Indigenous populations throughout the world are known to experience higher rates of ill-health compared with non-Indigenous populations, although there is a lack of quality data from low and middle-income countries [9]. Anderson et al. demonstrated that while Indigenous groups from a range of countries typically experience shorter life expectancy, higher infant and maternal mortality rates, lower levels of education and higher rates of chronic disease when compared with corresponding benchmark populations, this is not uniformly the case, and the magnitude of the discrepancy differs based on the study setting [10].

Analyses of historical data from the Spanish influenza pandemic of 1918 indicate that Indigenous populations were disproportionately affected throughout the United States, Canada, Nordic countries and the Pacific, with estimated mortality rates ranging from 90% among Alaskan Inuits to 1·3% among native Hawaiians [4]. These rates are significantly higher than the estimated mortality rates for the corresponding non-Indigenous populations (ranging from 0·20% to 0·79%) [4].

More advanced diagnostic technologies such as reverse transcription polymerase chain reaction (PCR) testing has enabled a high level of diagnostic accuracy to be achieved when testing for influenza in modern times, as was the case during the 2009 H1N1 pandemic (2009pH1N1). As demonstrated in a multi-country comparison by La Ruche et al., 2009pH1N1-associated hospitalisation and mortality among Indigenous populations was significantly higher when compared to benchmark populations in Canada (hospitalisation relative risk RR 5·7, mortality RR 3·4), the United States (hospitalisation RR 4·1, mortality RR 4·3), Brazil (hospitalisation RR 4·4), Australia (hospitalisation RR 7·7, mortality RR 5·1), New Zealand (hospitalisation RR 3·0) and New Caledonia (mortality RR 5·3) [3]. Almost one-hundred years following the Spanish influenza pandemic, the inequity in influenza disease burden with regard to Indigenous status remains stark.

It is therefore timely that a systematic review taking a global approach to the characterisation of influenza among Indigenous populations in both pandemic and inter-pandemic years be undertaken. The present study aimed to compare the rates of influenza-associated hospitalisation and mortality between Indigenous and non-Indigenous populations globally. This review has significant implications for informing vaccination policy, enhancing pandemic preparedness and addressing ethnic inequity.

Methods

Ethics statement

Formal ethics approval was not sought for this systematic review.

Search strategy and selection criteria

A systematic review and meta-analysis of literature published prior to 13 July 2021 was undertaken following the guidelines outlined in the PRISMA statement [11]. The review was registered with the International Prospective Register of Systematic Reviews (PROSPERO) prior to data extraction (Registration No.: CRD42017075598). The following electronic databases were searched; Pubmed, Medline, Embase, Cochrane Central Register of Controlled Trials and CINAHL. Reference lists of studies were also reviewed for additional relevant papers.

Based on the nominated Indigenous groups outlined by Anderson et al., [10] the following search terms were used (for full search strategy see Table A in S1 Text);

Indigenous OR Aborigin* OR native OR trib* OR First nation* OR Maori OR Inuit* OR Indians, North American OR (Torres Strait Island*) OR Dai OR Tibet* OR Mon OR Sherpa OR Rai OR Magar OR Tamang OR FATA OR Sami OR Nenet* OR Baka OR Pygm* OR Maasai OR Ijaw OR Fulani OR Metis OR Mapuche OR Kuna Yala OR (Embera Wounaan) OR Ngabe Bugle

AND

Influenza

AND

hospital* OR mortality OR death OR fatal*

Searches were undertaken by JB up to 13 June 2017 and were updated by JO from June 2017 to 13 July 2021. Selected data fields were abstracted and imported into the systematic review software Covidence [12]. Two independent reviewers assessed each record (JB, AW/MN for searches conducted to 13th June 2017 and JO, CH for the updated searches) using a two-step screen. First, articles were screened by title and abstract, and second by full text review. Disagreements were arbitrated by a third independent reviewer to reduce errors (KG).

To be included, studies had to be published in English, and contain data from primary observational research. Included studies had an extractable parameter such that a rate ratio was reported or could be calculated comparing influenza-associated hospitalisation and/or mortality rates between the Indigenous population and the corresponding benchmark population of a particular country or region. We included only studies with laboratory-confirmed influenza, or those deemed most likely to have used laboratory confirmation based on the study context. This was to ensure influenza alone was being studied, rather than other diseases with similar clinical presentations, such as pneumonia or other respiratory tract infections.

Single hospital-based studies that did not service states or regions with available denominator data, review articles, conference abstracts and studies which included cases based upon a clinical diagnosis of influenza alone were excluded. There were no timeframe or setting exclusions.

Data analysis

Microsoft Excel was used to extract relevant data. This was performed by JB or JO and verified by another author (AW/MN).

For included studies, abstracted data fields (where available) were: country and setting, nominated Indigenous population and comparison benchmark population, study period, age group, vaccination status, comorbidities, influenza strain and whether seasonal or pandemic, Indigenous and benchmark population hospitalisation rates, hospitalisation rate ratio, Indigenous and benchmark population mortality rates, mortality rate ratio, 95% confidence intervals, case fatality rates and sample size. Not all studies reported all these data, including some that did not report 95% confidence intervals for rates and rate ratios.

Two reviewers (MB and SH) independently assessed individual study quality and risk of bias using the Joanna Briggs Institute (JBI) critical appraisal checklist for cohort studies. Discrepancies in assessment were adjudicated by a third reviewer (KG).

Hospitalisation and mortality rates and rate ratios were reported and/or calculated based upon the number of events divided by the population at risk and presented per 100,000 person-months to enable comparison between studies that covered varying time periods. The rate ratio of influenza-associated hospitalisation and death in Indigenous compared to non-Indigenous populations for each country/region was reported and/or calculated. A global pooled rate ratio was not estimated due to hypothesised data heterogeneity and because each country and Indigenous group is distinct, limiting the impact of such a measure. However, where there were multiple studies originating from one country, a pooled rate ratio was calculated overall, and by pandemic or seasonal strain, if the necessary numerator and denominator figures were available. If not specified in the study, denominators were obtained from relevant, publicly available census data, which may have altered the rate ratios from those published in the original study. Pooled estimates, 95% confidence intervals and forest plots were generated using the statistical software STATA 15.1 [13]. A random effects model was chosen based upon the significant differences between studies in terms of geographical location and population. 95% confidence intervals (95% CI) that did not include the value 1 were considered statistically significant. The I2 estimate of heterogeneity was used to assess variability between studies.

Role of the funding source

There was no funding source for this study.

Results

Fig 1 depicts numbers of articles screened, assessed for eligibility and included in the review (see Table B in S1 Text for a full list of excluded articles). Thirty-six studies were included for data extraction and are summarised in Table C in S1 Text. Of the included studies, 15 (42%) were from Australia [1428], 10 (28%) were from the United States of America (USA) [2938], six (17%) were from New Zealand [3944], and four (11%) were from Canada [4548]. Only one (3%) was from a high-middle income country (Brazil) [49], and there were no included studies from low-middle or low-income countries.

Of the included studies, 21 (58%) had extractable data only for influenza-associated hospitalisation [1418,22,23,31,33,34,3844,4649] and five (14%) had extractable data only for influenza-associated mortality [21,29,30,35,36]. There were 10 studies (28%) with extractable data for both hospitalisation and mortality [19,20,2428,32,37,45]. Nearly three quarters of included studies (n = 26, 72%) analysed hospitalisations and/or deaths during the 2009pH1N1 [1720,2527,2933,3541,4449], while seven (19%) analysed hospitalisations and/or deaths from seasonal influenza [14,15,22,23,34,42,43] and four (11%) covered both seasonal and pandemic periods [16,21,24,28]. Of the 36 included studies, 28 (78%) had no age limitations [1732,3440,4446,48,49], while others considered children [1416,33,43], adults [41] or women of reproductive age [42,47]. Data used to calculate hospitalisation and mortality rates is provided in Table D in S1 Text.

The JBI critical appraisal tool findings are summarised in Table E and Table F in S1 Text. Indigenous and non-Indigenous groups were assessed from the same population with the exception of one study, which compared the Indigenous population in Alaska with the non-Indigenous population in the rest of the USA, indicating a higher risk of bias [33]. There was heterogeneity in the methods for assessing Indigenous status. Studies using maternal identification and population projections to identify Indigenous cases, as opposed to patient identification, were classified as having an unclear risk of bias [14,16,21,25,26]. Studies using ICD codes rather than laboratory data to identify influenza infections were also classified as unclear in category 6 of the JBI tool [14,2224,3335]. Category 4 of the JBI tool (regarding identification of confounding factors) identified a low risk of bias for 30/36 studies. Category 5 of the JBI tool (regarding strategies to address confounding factors) identified 25/36 studies with a low risk of bias. Using the composite of the JBI critical appraisal tool, no studies assessed were classified as having an overall high risk of bias.

Influenza-associated hospitalisation rates among Indigenous populations ranged from 0.8 hospitalisations per 100,000 person-months among Native Americans and Alaska Natives in the United States during the first wave (Spring/Summer) of the 2009pH1N1 [32], to 89.7 hospitalisations per 100,000 person-months among Aboriginal and Torres Strait Islander peoples in Australia during the 2009pH1N1 (Table 1) [17].

thumbnail
Table 1. Overall influenza-associated hospitalisation rates (HR) and hospitalisation rate ratios (HRR) (crude rates unless otherwise specified) for Indigenous peoples compared with a benchmark population.

https://doi.org/10.1371/journal.pgph.0001294.t001

A consistent pattern of statistically significant higher hospitalisation rates among Indigenous populations compared to benchmark populations was demonstrated (Table 1). The highest ethnic disparity was observed in Manitoba, Canada during the 2009pH1N1, whereby First Nations peoples were 16.1 (95% CI: 12·0–21·7) times more likely to be admitted to hospital for influenza compared with other Canadians [48]. The lowest hospitalisation rate ratio (HRR) was 1·2, observed in the United States over the seasonal influenza period 2001–2008 [34].

When observing pandemic influenza alone, HRRs comparing Indigenous to benchmark populations ranged from 1·4 in the United States [32], to 16·1 (95% CI: 12·0–21·7) in Canada [48]. When observing seasonal influenza alone, the highest disparity was observed among infants in Auckland, New Zealand, wherein Māori children were 11.1 (95% CI: 4.1–28.1) times more likely to be hospitalised for influenza compared with European and other children during the winter months of 2014–2016 [43]. The lowest seasonal influenza HRR was 1·2, observed in the USA over 2001–2008 [34].

For hospitalisations, the pooled overall influenza–associated HRR (Indigenous compared with the benchmark population) was 5·7 (95% CI: 2·7–12·0, n = 4 studies) for Canada, 5·2 (95% CI: 2.9–9.3, n = 3 studies) for New Zealand and 5.2 (95% CI: 4.2–6.4, n = 12 studies) for Australia (Fig 2).

thumbnail
Fig 2. Overall influenza-associated hospitalisation rate ratios (HRR) for Indigenous populations compared with a benchmark population by country.

https://doi.org/10.1371/journal.pgph.0001294.g002

Seven studies included data on seasonal influenza-associated hospitalisation (separate from pandemic influenza) [14,15,22,23,34,42,43], four (57%) of which were from Australia. For the three Australian studies with sufficient information, the pooled seasonal influenza HRR (Indigenous vs benchmark population) was 3.1 (95% CI: 2·7–3·5) (Fig 3). By contrast, for pandemic influenza, the pooled HRR in seven Australian studies was 6·2 (95% CI: 5·1–7·5). Heterogeneity was slightly higher among studies of pandemic influenza (I2 = 93·7%) compared with seasonal influenza (I2 = 79·1%).

thumbnail
Fig 3. Seasonal and pandemic influenza-associated hospitalisation rate ratios (HRR) from Australian studies for Indigenous populations compared with a benchmark population.

https://doi.org/10.1371/journal.pgph.0001294.g003

Globally, the lowest rate of influenza-associated mortality for an Indigenous population was 0.03 deaths per 100,000 person-months, observed among Indigenous Australians in the Northern Territory over the period 2007–2016 (Table 2) [28]. The highest Indigenous mortality rate was 1.6 deaths per 100,000 person-months among Indigenous Australians in North Queensland during the 2009pH1N1, however this was based on only five deaths over the study period [19].

thumbnail
Table 2. Overall influenza-associated mortality rates (MR) and mortality rate ratios (MRR) (crude rates unless otherwise specified) for Indigenous peoples compared with a benchmark population.

https://doi.org/10.1371/journal.pgph.0001294.t002

For benchmark populations, the lowest influenza-associated mortality rate was 0·0 deaths per 100,000 person-months, observed among benchmark populations of the United States [32] and Australia [24,28]. The highest mortality rate among benchmark populations was 0·5 deaths per 100,000 person-months, observed in North Queensland, Australia during the 2009pH1N1 [19] (Table 2).

Mortality rate ratios (MRR) tended to be greater than 1 (see Table 2), indicating an inequitable impact of influenza on Indigenous populations. The lower limit of the 95% CI was >1 for 12 of the 15 (80%) included studies [20,2430,32,35,36,45]; crossed one for two studies [19,37]; and was not reported for one study [21]. The greatest disparity in mortality was observed in Australia, whereby Indigenous Australians were 5·9 (95%CI: 3.6–9.1; age-standardised 5·7) times more likely to die from 2009pH1N1 compared with non-Indigenous Australians [24]. The lowest MRR was also observed in Australia (MRR = 1·1) which was an average MRR for years 2006–2013 [21]. For this study, when the MRR for 2009 was excluded (MRR = 3·3), the average MRR decreased to 0·79 (95% CI not provided).

The pooled influenza-associated MRR (Indigenous vs. benchmark populations) was 4.1 (95% CI: 3·0–5.7, n = 7 studies) in Australia and 3·3 (95%CI: 2.7–4.1, n = 5 studies) in the United States (Fig 4).

thumbnail
Fig 4. Overall influenza-associated mortality rate ratios (MRR) by country for Indigenous peoples compared with a benchmark population.

https://doi.org/10.1371/journal.pgph.0001294.g004

Discussion

This review demonstrates that Indigenous populations from Australia, New Zealand, the United States, Canada and Brazil endure a disproportionate burden of severe influenza, in terms of hospitalisations and/or mortality, compared with corresponding benchmark populations. This was consistent across included studies, with only two studies having rate ratio confidence intervals that crossed one (both of which included small numbers of influenza deaths: n = 35 and 5 respectively [19,37]. These findings are consistent with those demonstrated by La Ruche et al., who indicated consistently higher hospitalisation and mortality rates for Indigenous populations throughout the Americas and the Pacific during the first wave of the 2009pH1N1 [3].

This disparity between Indigenous and non-Indigenous populations in influenza-associated hospitalisation and mortality demonstrates a significant health inequity. Health inequities are systematic, avoidable and unnecessary differences in health between groups of people which exacerbate underlying social disadvantage [56]. For many global Indigenous populations, including those from Australia, Canada, New Zealand, the United States and Brazil, the experience of colonialism is the common factor driving health inequities [58]. While particular circumstances differ between populations, the effects of violent dispossession from traditional lands, policies of exclusion and ongoing experiences of racism and discrimination, particularly within the healthcare sector, continue to unjustly manifest in worse health outcomes for Indigenous peoples [5759].

Our findings from Australian studies demonstrate that the observed disparity between Indigenous and benchmark populations was more pronounced during 2009pH1N1 than with seasonal strains (HRRs 6·2; 95% CI: 5·1–7·5 and 3.1; 95% CI: 2·7–3·5 respectively). This is supported by the finding that the lowest rate ratios for both hospitalisation and mortality were observed among studies that included seasonal influenza periods [21,34]. The reason for this difference is not clear, however heterogeneity between the included studies was high, limiting the reliability of the pooled estimates. One possible explanation is differing demographic profiles between Indigenous and benchmark populations. Indigenous populations in Australia, Canada, New Zealand and the United States are younger compared to corresponding benchmark populations [51,6062] The 2009pH1N1 had a disproportionate effect on younger people, with the highest rates of notified disease among people aged 18–64 years, followed by children and adolescents aged 0–17 years [63]. In contrast, the majority of seasonal influenza hospitalisations and deaths occur among adults aged >65 years [1]. The age-standardisation of rates counteract this difference in population profile to an extent, although age-standardised rates were not consistently available.

Of note, data from the 2009pH1N1 dominated our findings, with only about one-third of included studies including seasonal influenza periods. Furthermore, the data on seasonal influenza was disproportionately found among Australian and New Zealand studies, with one study from the United States [34] and no studies from Canada or Brazil incorporating data on seasonal influenza. This reflects a limitation of our findings but also an important research gap in terms of sustaining influenza-related research during inter-pandemic periods to continue to understand priority populations for targeted public health interventions.

No eligible studies from low- and middle-income countries were identified, apart from one study from Brazil [49], an upper-middle income economy [64]. This, in part, reflects our inclusion criteria, which required publication in English, and laboratory-confirmation of influenza, as access to diagnostic technologies are limited in resource-poor settings. However, no eligible studies were identified from a number of other high-income countries with Indigenous populations (e.g. Norway, Denmark and Sweden) where legal prohibitions on the collection of ethnicity data exist [65]. The 2015 Sustainable Development Goals emphasised the need for more robust data collection which includes disaggregation by ethnicity, in order to achieve an accurate understanding of the health status of vulnerable populations to “leave no one behind” [66].

Hospitalisation and mortality rates were obtained from surveillance data, which is open to misclassification and outcome measurement bias. A number of included studies acknowledged that several regions within their country had imperfect reporting of ethnicity among cases. Similarly the data may have failed to account for secondary complications associated with influenza (for example bacterial pneumonia), whereby laboratory confirmation of the precipitating influenza infection may not have been sought. Consequently, the rates reported here likely underestimate the true extent of influenza-associated hospitalisation and mortality. Miscoding of data could have also led to missed cases of influenza, or accidental inclusion of other viruses with similar names (such as parainfluenza virus). Publication bias is also possible as studies that demonstrate a disparity between Indigenous and benchmark populations may be more likely to be published. However, for a number of the included studies, ethnic disparities were not the primary focus of the research.

The robust design of this review, in terms of its systematic approach and requirement for laboratory confirmation of influenza infection, is considered a strength. Included results are specific for influenza, rather than influenza and/or other respiratory illnesses. Previous studies, which fail to differentiate influenza from pneumonia, are generally more likely to document the effects of pneumonia as this typically accounts for 95% of undifferentiated pneumonia/influenza cases [35]. Specifically identifying influenza is worthwhile because of its unique virological properties in relation to pandemic potential and vaccine-preventability.

The disproportionate burden of influenza-associated hospitalisation and mortality among Indigenous populations is a significant global health inequity which must be addressed. The results of this review have far-reaching public health implications for global Indigenous communities as well as policy-makers, health practitioners and researchers. Efforts to reduce underlying socioeconomic inequalities, enhance health-care access, ensure appropriate and timely use of antiviral medication, and improve the design and uptake of influenza vaccines are key strategies to be considered. Moreover, the development of surveillance systems which accurately capture both influenza and ethnicity, particularly for less well represented low- and middle-income countries, are necessary to characterise the extent of the influenza disease burden among Indigenous populations globally. The findings from this review also suggest a more severe disparity occurred during pandemic periods of influenza, which emphasises the worldwide need to prioritise Indigenous populations in influenza pandemic response plans. Future research should prioritise quantifying the influenza disease burden among Indigenous populations of low and middle-income countries, as well as improving the effectiveness of influenza vaccines among Indigenous populations.

Research in context

Evidence before this study

Numerous studies comparing the health status of Indigenous populations with benchmark populations have demonstrated poorer health outcomes generally as well as specifically for influenza. However, most studies are based upon clinical diagnoses of influenza and focus on pandemic, rather than seasonal periods. To our knowledge, no global systematic review has compared influenza-specific hospitalisation and mortality between Indigenous and benchmark populations during seasonal and pandemic periods.

Added value of this study

This study provides a robust analysis of the available evidence relating to influenza hospitalisation and mortality for Indigenous populations compared with benchmark populations. Consistent across included studies, Indigenous populations from a number of countries endure higher rates of both hospitalisation and mortality due to influenza and this disparity may be more pronounced for pandemic, rather than seasonal influenza. This systematic review also highlighted the void in research from low- and middle-income countries, where influenza surveillance systems and diagnostic capacity may be less developed.

Implications of all the available evidence

Our findings have implications for influenza management strategies at both the population and individual level. Indigenous populations should be prioritised in influenza pandemic preparedness plans particularly with regard to the availability and uptake of influenza vaccines and antiviral medications. Policy-makers and health professionals should consider the wider contextual factors impacting upon the baseline level of health in Indigenous populations, and work together with Indigenous communities to achieve health equity. Future research should focus on characterising inequities between population groups in low- and middle-income countries as well as increasing the effectiveness of influenza vaccines among Indigenous populations.

Supporting information

S1 Text.

  • Table A: Search Strategy
  • Table B: List of excluded studies (from full text review)
  • Table C: Features of included studies
  • Table D: Notes about hospitalisation- and mortality-rate calculations
  • Table E: Quality assessment of included studies
  • Table F: JBI risk of bias assessment–comments.
  • References.

https://doi.org/10.1371/journal.pgph.0001294.s002

(DOC)

References

  1. 1. World Health Organization. Influenza (Seasonal)—Fact Sheet 2016 [cited on: 19/04/2017]. Available from: http://www.who.int/mediacentre/factsheets/fs211/en/.
  2. 2. Macias AE, McElhaney JE, Chaves SS, Nealon J, Nunes MC, Samson SI, et al. The disease burden of influenza beyond respiratory illness. Vaccine. 2021;39 Suppl 1:A6–A14. pmid:33041103
  3. 3. La Ruche G, Tarantola A, Barboza P, Vaillant L, Gueguen J, Gastellu-Etchegorry M. The 2009 pandemic H1N1 influenza and indigenous populations of the Americas and the Pacific. Euro surveillance: bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2009;14(42). pmid:19883543
  4. 4. Mamelund SE. Geography may explain adult mortality from the 1918–20 influenza pandemic. Epidemics. 2011;3(1):46–60. pmid:21420659
  5. 5. World Health Organization. WHO Public Health Research Agenda For Influenza—Biannual Progress Review and Report 2010–2011. 2013 [cited on: 21/04/2017]. Available from: http://www.who.int/influenza/resources/research/RA_Progress_Report_short.pdf?ua=1.
  6. 6. World Health Organization. Health of indigenous peoples—Fact Sheet 2007 [Cited on 28/06/2017]. Available from: http://www.who.int/mediacentre/factsheets/fs326/en/.
  7. 7. Martinez C. Study of the problem of discrimination against indigenous populations. Geneva: United Nations; 1986.
  8. 8. United Nations. United Nations Declaration on the Rights of Indienous Peoples 2008 [1/8/2017]. Available from: http://www.un.org/esa/socdev/unpfii/documents/DRIPS_en.pdf.
  9. 9. Gracey M, King M. Indigenous health part 1: determinants and disease patterns. The Lancet. 2009;374(9683):65–75. pmid:19577695
  10. 10. Anderson I, Robson B, Connolly M, Al-Yaman F, Bjertness E, King A, et al. Indigenous and tribal peoples’ health (The Lancet–Lowitja Institute Global Collaboration): a population study. The Lancet. 2016;388(10040):131–57. pmid:27108232
  11. 11. Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS medicine. 2009;6(7):e1000097. pmid:19621072
  12. 12. Mavergames C. Covidence (Systematic Review Software). 2013.
  13. 13. StataCorp LLC. Stata Statistical Software: Release 15.1. College Station, TX 2020.
  14. 14. Carville KS, Lehmann D, Hall G, Moore H, Richmond P, de Klerk N, et al. Infection is the major component of the disease burden in aboriginal and non-aboriginal Australian children: a population-based study. The Pediatric infectious disease journal. 2007;26(3):210–6. pmid:17484216
  15. 15. D’Onise K, Raupach JC. The burden of influenza in healthy children in South Australia. The Medical journal of Australia. 2008;188(9):510–3. pmid:18459921
  16. 16. Fathima P, Blyth CC, Lehmann D, Lim FJ, Abdalla T, De Klerk N, et al. The impact of pneumococcal vaccination on bacterial and viral pneumonia in Western Australian children: record linkage cohort study of 469589 births, 1996–2012. Clinical Infectious Diseases. 2018;66(7):1075–85. pmid:29069315
  17. 17. Flint SM, Davis JS, Su JY, Oliver-Landry EP, Rogers BA, Goldstein A, et al. Disproportionate impact of pandemic (H1N1) 2009 influenza on Indigenous people in the Top End of Australia’s Northern Territory. Medical Journal of Australia. 2010;192(10):617–22. pmid:20477746
  18. 18. Goggin LS, Carcione D, Mak DB, Dowse GK, Giele CM, Smith DW, et al. Chronic disease and hospitalisation for pandemic (H1N1) 2009 influenza in Indigenous and non-Indigenous Western Australians. Communicable Diseases Intelligence. 2011;35(2):172–6. pmid:22010511
  19. 19. Harris PN, Dixit R, Francis F, Buettner PG, Leahy C, Burgher B, et al. Pandemic influenza H1N1 2009 in north Queensland—risk factors for admission in a region with a large indigenous population. Communicable Diseases Intelligence. 2010;34(2):102–9. pmid:20677419
  20. 20. Kelly H, Mercer G, Cheng A. Quantifying the risk of pandemic influenza in pregnancy and indigenous people in Australia in 2009. Euro surveillance: bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2009;14(50). pmid:20070939
  21. 21. Li-Kim-Moy J, Yin JK, Patel C, Beard FH, Chiu C, Macartney KK, et al. Australian vaccine preventable disease epidemiological review series: Influenza 2006 to 2015. Communicable diseases intelligence quarterly report. 2016;40(4):E482–e95. pmid:28043223
  22. 22. Menzies R, McIntyre P, Beard F. Vaccine preventable diseases and vaccination coverage in Aboriginal and Torres Strait Islander people, Australia, 1999 to 2002. Communicable diseases intelligence quarterly report. 2004;28(2):127–59. pmid:15460950
  23. 23. Menzies R, Turnour C, Chiu C, McIntyre P. Vaccine preventable diseases and vaccination coverage in Aboriginal and Torres Strait Islander people, Australia 2003 to 2006. Communicable diseases intelligence quarterly report. 2008;32 Suppl:S2–67. pmid:18711998
  24. 24. Naidu L, Chiu C, Habig A, Lowbridge C, Jayasinghe S, Wang H, et al. Vaccine preventable diseases and vaccination coverage in Aboriginal and Torres Strait Islander people, Australia 2006–2010. Communicable diseases intelligence quarterly report. 2013;37 Suppl:S1–95. pmid:24410428
  25. 25. New South Wales Public Health Network. Progression and impact of the first winter wave of the 2009 pandemic H1N1 influenza in New South Wales, Australia. Eurosurveillance. 2009;14(42):19365. pmid:19883546
  26. 26. Pennington K, Owen R, Mun J. Annual Report of the National Influenza Surveillance Scheme, 2009. Communicable Diseases Intelligence. 2017;41(4). pmid:29864390
  27. 27. Rudge S, Massey PD. Responding to pandemic (H1N1) 2009 influenza in Aboriginal communities in NSW through collaboration between NSW Health and the Aboriginal community-controlled health sector. New South Wales public health bulletin. 2010;21(1–2):26–9. pmid:20374691
  28. 28. Weinman AL, Sullivan SG, Vijaykrishna D, Markey P, Levy A, Miller A, et al. Epidemiological trends in notified influenza cases in Australia’s Northern Territory, 2007‐2016. Influenza and other respiratory viruses. 2020;14(5):541–50. pmid:32445270
  29. 29. Brooks EG, Bryce CH, Avery C, Smelser C, Thompson D, Nolte KB. 2009 H1N1 Fatalities: The New Mexico Experience. Journal of Forensic Sciences. 2012;57(6):1512–8. pmid:22571830
  30. 30. Centers for Disease Control and Prevention. Deaths related to 2009 pandemic influenza A (H1N1) among American Indian/Alaska Natives—12 states, 2009. MMWR—Morbidity & Mortality Weekly Report. 2009;58(48):1341–4. pmid:20010508
  31. 31. Chowell G, Ayala A, Berisha V, Viboud C, Schumacher M. Risk factors for mortality among 2009 A/H1N1 influenza hospitalizations in Maricopa County, Arizona, April 2009 to March 2010. Computational and Mathematical Methods in Medicine. 2012;2012 (no pagination)(914196). pmid:22844347
  32. 32. Dee DL, Bensyl DM, Gindler J, Truman BI, Allen BG, D’Mello T, et al. Racial and Ethnic Disparities in Hospitalizations and Deaths Associated with 2009 Pandemic Influenza A (H1N1) Virus Infections in the United States. Annals of Epidemiology. 2011;21(8):623–30. pmid:21737049
  33. 33. Foote EM, Singleton RJ, Holman RC, Seeman SM, Steiner CA, Bartholomew M, et al. Lower respiratory tract infection hospitalizations among American Indian/Alaska Native children and the general United States child population. International journal of circumpolar health. 2015;74:29256. pmid:26547082
  34. 34. Gounder PP, Callinan LS, Holman RC, Cheng PY, Bruce MG, Redd JT, et al. Influenza hospitalizations among American Indian/Alaska Native people and in the United States general population. Open Forum Infectious Diseases. 2014;1(1). pmid:25734102
  35. 35. Groom AV, Hennessy TW, Singleton RJ, Butler JC, Holve S, Cheek JE. Pneumonia and Influenza Mortality Among American Indian and Alaska Native People, 1990–2009. American Journal of Public Health. 2014(S3):S460–9. pmid:24754620
  36. 36. Hennessy TW, Bruden D, Castrodale L, Komatsu K, Erhart LM, Thompson D, et al. A case-control study of risk factors for death from 2009 pandemic influenza A(H1N1): is American Indian racial status an independent risk factor? Epidemiology & Infection. 2016;144(2):315–24. pmid:26118767
  37. 37. Thompson DL, Jungk J, Hancock E, Smelser C, Landen M, Nichols M, et al. Risk Factors for 2009 Pandemic Influenza A (H1N1)-Related Hospitalization and Death Among Racial/Ethnic Groups in New Mexico. American Journal of Public Health. 2011;101(9):1776–84. pmid:21778495
  38. 38. Wenger JD, Castrodale LJ, Bruden DL, Keck JW, Zulz T, Bruce MG, et al. 2009 pandemic influenza a H1N1 in Alaska: Temporal and geographic characteristics of spread and increased risk of hospitalization among Alaska native and Asian/Pacific islander people. Clinical Infectious Diseases. 2011;52(SUPPL. 1):S189–S97. pmid:21342894
  39. 39. Baker MG, Wilson N, Huang QS, Paine S, Lopez L, Bandaranayake D, et al. Pandemic influenza A(H1N1)v in New Zealand: the experience from April to August 2009. Euro Surveillance: Bulletin Europeen sur les Maladies Transmissibles = European Communicable Disease Bulletin. 2009;14(34):27.
  40. 40. Bandaranayake D, Jacobs M, Baker M, Hunt D, Wood T, Bissielo A, et al. The second wave of 2009 pandemic influenza a(H1N1) in New Zealand, January-October 2010. Eurosurveillance. 2011;16(6). pmid:21329643
  41. 41. Dee S, Jayathissa S. Clinical and epidemiological characteristics of the hospitalised patients due to pandemic H1N1 2009 viral infection: Experience at Hutt Hospital, New Zealand. New Zealand Medical Journal. 2010;123(1312):45–53.
  42. 42. Prasad N, Huang QS, Wood T, Aminisani N, McArthur C, Baker MG, et al. Influenza-associated outcomes among pregnant, postpartum, and nonpregnant women of reproductive age. The Journal of infectious diseases. 2019;219(12):1893–903. pmid:30690449
  43. 43. Prasad N, Trenholme AA, Huang QS, Duque J, Grant CC, Newbern EC. Respiratory virus-related emergency department visits and hospitalizations among infants in New Zealand. The Pediatric infectious disease journal. 2020;39(8):e176–e82. pmid:32675757
  44. 44. Verrall A, Norton K, Rooker S, Dee S, Olsen L, Tan CE, et al. Hospitalizations for pandemic (H1N1) 2009 among Maori and Pacific Islanders, New Zealand. Emerging infectious diseases. 2010;16(1):100–2. pmid:20031050
  45. 45. Helferty M, Vachon J, Tarasuk J, Rodin R, Spika J, Pelletier L. Incidence of hospital admissions and severe outcomes during the first and second waves of pandemic (H1N1) 2009. Cmaj. 2010;182(18):1981–7. pmid:21059773
  46. 46. Mostaco-Guidolin LC, Towers SM, Buckeridge DL, Moghadas SM. Age distribution of infection and hospitalization among Canadian First Nations populations during the 2009 H1N1 pandemic. American journal of public health. 2013;103(2):e39–44. pmid:23237152
  47. 47. Rolland-Harris E, Vachon J, Kropp R, Frood J, Morris K, Pelletier L, et al. Hospitalization of pregnant women with pandemic A(H1N1) 2009 influenza in Canada. Epidemiology & Infection. 2012;140(7):1316–27. pmid:21920067
  48. 48. Zarychanski R, Stuart TL, Kumar A, Doucette S, Elliott L, Kettner J, et al. Correlates of severe disease in patients with 2009 pandemic influenza (H1N1) virus infection. CMAJ: Canadian Medical Association Journal. 2010;182(3):257–64.
  49. 49. Lenzi L, de Mello AM, da Silva LR, Grochocki MHC, Pontarolo R. Pandemic influenza A (H1N1) 2009: Risk factors for hospitalization. Jornal Brasileiro de Pneumologia. 2012;38(1):57–65. pmid:22407041
  50. 50. Australian Bureau of Statistics. 2011 Census Quickstats 2017 [cited on: 29/9/2017]. Available from: http://www.censusdata.abs.gov.au/census_services/getproduct/census/2011/quickstat/5?opendocument.
  51. 51. Statistics Canada. Aboriginal Peoples in Canada: First Nations People, Métis and Inuit 2016 [cited on: 28/9/2017]. Available from: http://www12.statcan.gc.ca/nhs-enm/2011/as-sa/99-011-x/99-011-x2011001-eng.cfm.
  52. 52. Instituto Brasileiro De Geografia e Estatistica (IBGE). Tendências Demográficas—Uma análise dos indígenas com base nos resultados da amostra dos Censos Demográficos 1991 e 2000. Rio de Janeiro; 2005.
  53. 53. Australian Bureau of Statistics. 2006 Census QuickStats 2017 [cited on: 31/10/2017]. Available from: http://www.censusdata.abs.gov.au/census_services/getproduct/census/2006/quickstat/1?opendocument.
  54. 54. Statistics Canada. Selected language characteristics, Aboriginal identity, age groups and sex for the population of Canada, Provinces, Territories and Census Metropolitan Areas, 2006 Census. Cat no. 97-558-XCB2006016 Ottawa: Statistics Canada; 2008 [Available from: https://www12.statcan.gc.ca/census-recensement/2006/dp-pd/tbt/Rp-eng.cfm?LANG=E&APATH=3&DETAIL=1&DIM=0&FL=A&FREE=1&GC=0&GID=0&GK=0&GRP=1&PID=89150&PRID=0&PTYPE=88971&S=0&SHOWALL=No&SUB=0&Temporal=2006&THEME=73&VID=0&VNAMEE=&VNAMEF=.
  55. 55. U.S. Census Bureau. 2010 Census Interactive Population Search 2011 [cited on: 15/9/2017]. Available from: http://www12.statcan.gc.ca/census-recensement/2011/rt-td/index-eng.cfm?TABID=6.
  56. 56. Braveman P, Gruskin S. Defining equity in health. Journal of Epidemiology and Community Health 2003;57:254–258. pmid:12646539
  57. 57. Reading CL, Wien F. Health inequalities and the social determinants of Aboriginal peoples’ health: National Collaborating Centre for Aboriginal Health Prince George, BC; 2009.
  58. 58. Reid P, Cormack D, Paine SJ. Colonial histories, racism and health—The experience of Māori and Indigenous peoples. Public Health. 2019;172:119–24.
  59. 59. Hamed S, Bradby H, Ahlberg BM et al. Racism in healthcare: a scoping review. BMC Public Health 2022;22(1):1–22.
  60. 60. Census Bureau U.S. We the People: American Indians and Alaska Natives in the United States 2006 [cited on: 19/10/2017]. Available from: https://www.census.gov/content/dam/Census/library/publications/2006/dec/censr-28.pdf.
  61. 61. Statistics New Zealand. 2013 Census QuickStats about Māori 2013 [cited on: 19/10/2017]. Available from: http://www.stats.govt.nz/Census/2013-census/profile-and-summary-reports/quickstats-about-maori-english.aspx.
  62. 62. Australian Bureau of Statistics. 2016 Census Data Summary; Aboriginal and Torres Strait Islander Population 2017 [cited on: 19/10/2017]. Available from: http://www.ausstats.abs.gov.au/Ausstats/subscriber.nsf/0/C1DE83F220B089E3CA2581470023C96E/$File/aboriginal%20and%20torres%20strait%20islander%20population,%202016%20census%20data%20summary.pdf.
  63. 63. Centers for Disease Control and Prevention. Flu-related hospitalizations and deaths in the United States from APril 2009—January 30, 2010 2010 [Cited on: 19/10/2017]. Available from: https://www.cdc.gov/H1N1flu/hosp_deaths_ahdra.htm.
  64. 64. The World Bank. World bank Country and Lending Groups 2017 [cited on: 19/10/2017]. Available from: https://datahelpdesk.worldbank.org/knowledgebase/articles/906519.
  65. 65. Simon P. Collecting ethnic statistics in Europe: a review. Ethnic and Racial Studies. 2012;35(8):1366–91.
  66. 66. World Health Organization Commission on Social Determinants of Health. Closing the gap in a generation: health equity through action on the social determinants of health: Commission on Social Determinants of Health final report: World Health Organization; 2008.